*most significant finding
- increased synthesis/cell proliferation
- cell membrane damage
- cell death
- defective/slow blood clearance
Level increased can = extent of injury
Isoenzyme = greater tiss specificity
Enzyme profiles
1) tissue of origin
2) isoenz pattern in tiss
3) timing in relation to disease
4) lab availability
Normal variations of enzyme levels
1) Age/sex variation in reference range (ALP higher in adolescents)
2) Race (CK higher in afro-Caribbean)
3) Analytical interference (transaminases & LDH - haemolysis from red cells)
4) Renal failure (Amylase increased, as excreted renal-ly)
5) 'Macro enzymes' - binding of enzyme to immunoglobulin - lowers rate of degradation
- primary protein (immunoglobulin) disease eg myeloma
- temp
- *CK & AMY
- = req alt of Ix w/ documentation
2) isoenz pattern in tiss
3) timing in relation to disease
4) lab availability
Normal variations of enzyme levels
1) Age/sex variation in reference range (ALP higher in adolescents)
2) Race (CK higher in afro-Caribbean)
3) Analytical interference (transaminases & LDH - haemolysis from red cells)
4) Renal failure (Amylase increased, as excreted renal-ly)
5) 'Macro enzymes' - binding of enzyme to immunoglobulin - lowers rate of degradation
- primary protein (immunoglobulin) disease eg myeloma
- temp
- *CK & AMY
- = req alt of Ix w/ documentation
Dx
MI
CK & CK-MB
troponin (non-enzyme)
CK & CK-MB
troponin (non-enzyme)
x transamimases/LDH
Liver
ALT
ALP
GGT
Pancreatitis
Amy
Liver
ALT
ALP
GGT
Pancreatitis
Amy
Skeletal
CK for muscles
ALP for bone
ALP for bone
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